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Predictors of survival in patients with established cirrhosis and hepatocellular carcinoma treated with sorafenib
Authors:Andrea L Inghilesi  Donatella Gallori  Lorenzo Antonuzzo  Paolo Forte  Daniela Tomcikova  Umberto Arena  Stefano Colagrande  Silvia Pradella  Bernardo Fani  Elena Gianni  Luca Boni  Giacomo Laffi  Francesco Di Costanzo  Fabio Marra
Affiliation:Andrea L Inghilesi;Donatella Gallori;Lorenzo Antonuzzo;Paolo Forte;Daniela Tomcikova;Umberto Arena;Stefano Colagrande;Silvia Pradella;Bernardo Fani;Elena Gianni;Luca Boni;Giacomo Laffi;Francesco Di Costanzo;Fabio Marra;Dipartimento di Medicina Sperimentale e Clinica,Università degli Studi di Firenze;Oncologia Medica,Azienda Ospedaliero-Universitaria Careggi;Gastroenterologia 2,Azienda Ospedaliero-Universitaria Careggi;Centro per il Coordinamento delle Sperimentazioni Cliniche,Istituto Toscano Tumori,and Azienda Ospedaliero-Universitaria Careggi;Dipartimento di Scienze Biomediche,Sperimentali e Cliniche,Università degli Studi di Firenze;
Abstract:AIM: To investigate in greater detail the efficacy and safety of sorafenib for the treatment of hepatocellular carcinoma (HCC) in patients with established cirrhosis.METHODS: From October 2009 to July 2012 patients with an established diagnosis of cirrhosis and HCC treated with sorafenib were consecutively enrolled. According to the Barcelona Clinic Liver Cancer (BCLC) classification, patients were in the advanced stage (BCLC-C) or in the intermediate stage (BCLC-B) but unfit or unresponsive to other therapeutic strategies. Treatment was evaluated performing a 4-phase computed tomography or magnetic resonance imaging scan every 2-3 mo, and analyzed according to the modified Response Evaluation Criteria in Solid Tumors. Sorafenib was administered at 800 mg/d, until radiological progression or occurrence of unacceptable adverse events (AEs). Univariate and multivariate analyses identified predictors of 16-wk clinical benefit and overall survival.RESULTS: Forty-four patients were enrolled, 15 had intermediate HCC and 14 a Child-Pugh score of B7. AEs caused treatment interruption in 19 patients (43%), and median treatment duration was shorter in this subset (5 wk vs 19 wk, P < 0.001) and in the BCLC-C subgroup (13 wk vs 40 wk, P = 0.015). No significant differences in the reason for treatment interruption or in treatment duration were found comparing patients in Child-Pugh class A vs B or in patients older or younger than 70 years. After 16 wk of treatment, 18 patients (41%) had stable disease or partial response. Patients with viral infection or BCLC-C were at higher risk of disease progression. ECOG, extrahepatic spread, macrovascular invasion, alpha-fetoprotein or alkaline phosphatase levels at admission were independent predictors of overall survival.CONCLUSION: In patients with cirrhosis and HCC treated with sorafenib, AEs are a common cause of early treatment withdrawal. Vascular invasion and extrahepatic spread condition early response to treatment and survival. Baseline biochemical parameters may be helpful to identify patients at higher risk of shorter overall survival.
Keywords:Hepatocellular carcinoma   Sorafenib   Cirrhosis   Adverse events   Barcelona Clinic Liver Cancer
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